ClinVar Miner

List of variants in gene GLIS3 reported as likely benign for abdominal and pelvic region disorder

Included ClinVar conditions (891):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 23
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HGVS dbSNP
NM_001042413.1(GLIS3):c.*1602T>G rs80030970
NM_001042413.1(GLIS3):c.*1760T>G rs116077269
NM_001042413.1(GLIS3):c.*1827T>G rs16919705
NM_001042413.1(GLIS3):c.*1832A>G rs10116901
NM_001042413.1(GLIS3):c.*2673dupA rs147364042
NM_001042413.1(GLIS3):c.*2806G>A rs12351289
NM_001042413.1(GLIS3):c.*2813C>T rs77896717
NM_001042413.1(GLIS3):c.*2840dupA rs142133114
NM_001042413.1(GLIS3):c.*2944T>C rs2297324
NM_001042413.1(GLIS3):c.*3012G>C rs35359206
NM_001042413.1(GLIS3):c.*3218A>C rs73640770
NM_001042413.1(GLIS3):c.*3377delA rs202118987
NM_001042413.1(GLIS3):c.*3409G>A rs115222174
NM_001042413.1(GLIS3):c.*3692A>T rs75958174
NM_001042413.1(GLIS3):c.*663_*664dupAA rs5896025
NM_001042413.1(GLIS3):c.*711C>G rs4997836
NM_001042413.1(GLIS3):c.-270C>A rs73641408
NM_001042413.1(GLIS3):c.-681C>T rs138857227
NM_001042413.1(GLIS3):c.1126C>T (p.Pro376Ser) rs76342955
NM_001042413.1(GLIS3):c.1216G>T (p.Gly406Cys) rs75462592
NM_001042413.1(GLIS3):c.171C>T (p.Asn57=) rs117802495
NM_152629.3(GLIS3):c.1071C>A (p.Asp357Glu) rs148199056
NM_152629.3(GLIS3):c.2221C>T (p.Leu741Phe) rs76094493

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